93634-60-7Relevant articles and documents
Stereoselective synthesis of dehydroamino acids using malonic acid half oxyester and aromatic aldehydes
Singjunla, Yuttapong,Colombano, Silvia,Baudoux, Jér?me,Rouden, Jacques
, p. 2369 - 2375 (2016/04/26)
An efficient and direct approach was developed for the synthesis of α,β-dehydroamino acid derivatives with a broad range of substrates. Amido-substituted Malonic Acid Half Oxyesters (MAHOs) have proven to be excellent partners of various aromatic aldehyde
The use of cyclohexyl isocyanide in the esterification of N-benzoyl α-amino acids derivatives
Hassanabadi, Alireza,Anary-Abbasinejad, Mohammad,Niri, Atefeh Ahmadi,Feizpoor, Rozita
, p. 468 - 470 (2011/11/29)
The N-benzoyl of α,β-dehydroamino acids that were obtained by condensation of N-benzoylglycine and an aldehyde, were esterified with an alcohol in high yield using cyclohexyl isocyanide to activate the carboxylic acid under neutral conditions.
TRIETHYLAMINE, ETHANOL- MEDIATED DISCIPLINED REACTIONS OF S-BENZYLISOTHIOURONIUM CHLORIDE WITH UNSATURATED 2-OXAZOLIN-5-ONES: SYNTHESIS OF (Z)-2-AMINO-4-ARYLMETHYLENE-2-IMIDAZOLIN-5-ONES, 5-BENZOYLAMINO-2-BENZYLTHIO-6-OXO-4,4-SPIROCYCLOHEXYL-1,4,5,6-TETRA
Mukerjee, Arya K.,Joseph, Kiran,Homami, Seyed-Saied,Tikdari, Ahmad M.
, p. 1317 - 1325 (2007/10/02)
Triethylamine-mediated condensation of S-benzylisothiouronium chloride with (Z)-4-arylmethylene-2-phenyl-2-oxazolin-5-ones (4) in ethanol gives (Z)-2-amino-4-arylmethylene-2-imidazolin-5-ones (7), whereas the similar reaction with 4-cyclohexylidene-2-phen
